A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1675788



Internal ID15533296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26558113..26745817hg38UCSC Ensembl
Innerchr15:26803260..26990964hg19UCSC Ensembl
Innerchr15:24354353..24542057hg18UCSC Ensembl
Innerchr15:24350621..24538325hg16UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38187705
hg19187705
hg18187705
hg16187705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469894
Supporting Variants
Samples
Known GenesGABRB3
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nssv1675788
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer